Diagnosing familial platelet disorder with predisposition to myeloid malignancy: Lessons learned from a germline whole‐gene deletion of <scp><i>RUNX1</i></scp>-Reference-Cited by-同舟云学术

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Diagnosing familial platelet disorder with predisposition to myeloid malignancy: Lessons learned from a germline whole‐gene deletion of RUNX1

Published:2023-11-12 Issue:1 Volume:46 Page:203-206
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hematology

Author:

Cliburn John A.¹^ORCID,Uy Jann C.²,Swift Sharon³,Liesveld Jane L.³,Iqbal M. Anwar²,Jajosky Audrey N.²,Becker Michael W.³

Affiliation:

1. School of Medicine and Dentistry University of Rochester Rochester New York USA

2. Department of Pathology, Laboratory Medicine University of Rochester Medical Center Rochester New York USA

3. Department of Medicine, Division of Hematology and Oncology University of Rochester Medical Center, Wilmot Cancer Institute Rochester New York USA

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.14199

Reference12 articles.

1. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

2. Molecular Basis of Hematological Disease Caused by Inherited or Acquired RUNX1 Mutations

3. RUNX1 germline variants in RUNX1-mutant AML: how frequent?

4. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia

5. The RUNX1 Database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

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